Variant #0000000021 (NC_000017.10:g.56798128A>G, NM_058216.2:c.859A>G (RAD51C))

Chromosome 17
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Probably does not affect function
DNA change (genomic) (Relative to hg19 / GRCh37) g.56798128A>G
Reference -
DB-ID RAD51C_000002
Frequency -
Average frequency (gnomAD v.2.1.1) 0.00555 View details
Owner Florian Bayersdorfer
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Florian Bayersdorfer
Date created 2017-05-15 10:23:49 +00:00 (UTC)
Date last edited 2023-07-18 10:54:08 +00:00 (UTC)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RAD51C NM_058216.2 -?/-? 6 c.859A>G r.(?) p.(Thr287Ala)